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Principal Statistical Programmer - Remote, Office or Hybrid - UK, Liverpool
Client: Veramed
Location: Liverpool, United Kingdom
Job Category: Other
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EU work permit required: Yes
Job Views:
4
Posted:
26.06.2025
Expiry Date:
10.08.2025
Job Description:
Veramed prides itself on providing high-quality statistics and programming consultancy, and offering an excellent working environment with support and training for career growth.
We are seeking a Principal Statistical Programmer for a permanent role in the UK. The position offers flexible working options, training, support, and a competitive package.
The role involves providing programming support across various projects and therapeutic areas. The Senior or Principal Programmer may also have supervisory responsibilities, including line and project management.
Key Responsibilities
The tasks include, but are not limited to:
* Review of clinical trial documents such as protocols, SAPs, CRFs, and CSRs
* Authoring, reviewing, and approving study TFL shells and dataset specifications
* Authoring, validating, and documenting SAS programs, ensuring good programming practices
* Identifying data issues and outliers
* Reviewing CDISC Validation reports
* Resolving data and standards issues or escalating as needed
* Staying updated on emerging standards and their impact on trials
* Maintaining proficiency in SAS and awareness of developments
* Managing study documentation to ensure audit readiness
People Management
Line management of statisticians, programmers, and technical staff, including coaching, mentoring, and career development. Responsible for onboarding new staff and providing technical leadership.
Project Management
Oversee key projects, maintain project plans, manage resources, scope, risks, and budgets, and handle client expectations and issues.
General Responsibilities
Lead meetings, present updates, share knowledge, ensure compliance, build collaborative relationships, and develop internal training.
Qualifications
BSc, MSc, or PhD in a numerical discipline or relevant industry experience, with at least 6 years of relevant experience.
Additional Requirements
Understanding of clinical drug development, disease areas, endpoints, and study designs.
What to Expect
* A supportive and friendly work environment
* Open-door management policy for development
* A unique CRO with innovative staff and project management
* Opportunities for role ownership and skill development
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